| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:29073532-29073848 | Common:2; Rare:100 | ||||
| chr21:29298620-29298935 | Common:2; Rare:124 | ||||
| chr21:32279019-32279212 | Common:3; Rare:83 | ||||
| chr21:32392967-32393156 | Common:2; Rare:80 | ||||
| chr21:33324866-33325035 | Common:4; Rare:69 | ||||
| chr21:33479845-33480158 | Rare:105 | ||||
| chr21:33542821-33543092 | Common:2; Rare:96 | ||||
| chr21:36134888-36135178 | Common:1; Rare:73 | ||||
| chr21:37073019-37073357 | Common:5; Rare:133 | ||||
| chr21:39445751-39445870 | Common:3; Rare:37 | ||||
| chr21:41361917-41362039 | Common:1; Rare:16 | ||||
| chr21:41426151-41426325 | Common:1; Rare:29 | ||||
| chr21:42879505-42879680 | Common:3; Rare:61 | ||||
| chr21:43659485-43659570 | Common:1; Rare:25 | ||||
| chr21:43776235-43776492 | Common:5; Rare:95; Clinvar:4; Clinvar (benign):10; Clinvar (pathogenic):2 |